Canonical Allele Identifier: CA1468148143

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419532A= , CM000666.2:g.73419532A=	GRCh38
NC_000004.11:g.74285249A= , CM000666.1:g.74285249A=	GRCh37
NC_000004.10:g.74504113A=	NCBI36
NG_009291.1:g.20278A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1678A= MANE Select	ENSP00000295897.4:p.Lys560=
ENST00000295897.8:c.1678A=	ENSP00000295897.4:p.Lys560=
ENST00000401494.7:c.1333A=	ENSP00000384695.3:p.Lys445=
ENST00000415165.6:c.1102A=	ENSP00000401820.2:p.Lys368=
ENST00000476441.6:c.*957A=	ENSP00000423727.1:n.*957A=
ENST00000486939.1:n.332A=
ENST00000503124.5:c.1228A=	ENSP00000421027.1:p.Lys410=
ENST00000505649.5:n.1225A=
ENST00000508932.5:n.175+77A=
ENST00000509063.5:c.1678A=	ENSP00000422784.1:p.Lys560=
ENST00000511370.1:c.1211A=
ENST00000621085.4:c.1039A=	ENSP00000483421.1:p.Lys347=
ENST00000621628.4:c.1039A=	ENSP00000480485.1:p.Lys347=
NM_000477.5:c.1678A=	NP_000468.1:p.Lys560=
NM_000477.6:c.1678A=	NP_000468.1:p.Lys560=
NM_000477.7:c.1678A= MANE Select	NP_000468.1:p.Lys560=